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Updated: May 20, 2026

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
Congenital adrenal hyperplasia masquerading as periodic paralysis in an adolescent girl
Anjali Sathya1, R Ganesan, Arun Kumar
1Department of Endocrinology, Vijaya Hospital, 175, NSK Salai, Saligramam, Vadapalani, Chennai 600026, Tamil Nadu, India. anjalisathyab@yahoo.co.in
Abstract:
Congenital adrenal hyperplasia is an uncommon diagnosis in routine clinical practice. 21-hydroxylase deficiency, which is its most common subtype, may be diagnosed at birth in a female infant by virilisation or by features of salt wasting in both genders. However, other uncommon subtypes of this condition such as 17-alpha-hydroxylase deficiency, 11-beta-hydroxylase deficiency may present much later in adolescence or adulthood. A high index of suspicion is necessary when evaluating children with hypertension, hypokalaemia, metabolic alkalosis or sexual infantilism.
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